Canonical Allele Identifier: CA1619378914

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951139T= , CM000668.2:g.31951139T=	GRCh38
NC_000006.11:g.31918916T= , CM000668.1:g.31918916T=	GRCh37
NC_000006.10:g.32026895T=	NCBI36
NG_008191.1:g.10196T= , LRG_136:g.10196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-58T=
ENST00000483004.2:c.1640-5T=	ENSP00000419887.2:n.1640-5T=
ENST00000698628.1:c.1625-5T=	ENSP00000513848.1:n.1625-5T=
ENST00000698629.1:n.2128-58T=
ENST00000698630.1:n.2572-5T=
ENST00000698631.1:n.2573-5T=
ENST00000698632.1:n.3656T=
ENST00000698633.1:n.3546T=
ENST00000425368.7:c.1856-5T= MANE Select	ENSP00000416561.2:n.1856-5T=
ENST00000425368.6:c.1856-5T=	ENSP00000416561.2:n.1856-5T=
ENST00000456570.5:c.3362-5T=	ENSP00000410815.1:n.3362-5T=
ENST00000467360.1:n.982-5T=
ENST00000477310.1:c.2909-5T=	ENSP00000418996.1:n.2909-5T=
ENST00000482312.1:n.266T=
ENST00000483004.1:c.478-5T=
NM_001710.5:c.1856-5T= , LRG_136t1:c.1856-5T=	NP_001701.2:n.1856-5T=
NM_001710.6:c.1856-5T= MANE Select	NP_001701.2:n.1856-5T=